Benzoyl Peroxide
- Product NDC
- 68071-2307
- 11-digit product format
- 680712307
- Labeler code
- 68071
- Product ID
- 68071-2307_1d78819d-c76c-7ba4-e063-6394a90a404d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzoyl Peroxide
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- M014
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2015-01-20
- Substance
- BENZOYL PEROXIDE
- Active strength
- 50 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Benzoyl Peroxide
- Brand name suffix
- Acne Medication
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZOYL PEROXIDE | 50 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | W9WZN9A0GM |
| Rxcui | 308694 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68071-2307-5 | Benzoyl PeroxideAcne Medication | 42.5 mL in 1 TUBE | GEL | 42.5 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2307 | BENZOYL PEROXIDE ACNE MEDICATION (BENZOYL PEROXIDE) GEL [NUCARE PHARMACEUTICALS,INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20240726_b55acec6-5a4d-08b7-e053-2995a90a0f74.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2307-5 | 68071230705 | 42.5 mL in 1 TUBE (68071-2307-5) | 42.5 ml | 2020-11-30 | 0000-00-00 | No | No | Current |